Visitor Monitoring Drug Details: ACCUTANE
 
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Drug Details

Drug Name: ACCUTANE
FDA Application No: (NDA) 018662
Active Ingredient(s): ISOTRETINOIN
Company: HLR
Original Approval or Tentative Approval Date: May 7, 1982
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ACCUTANE ISOTRETINOIN10MGCAPSULE; ORAL Prescription No AB
ACCUTANE ISOTRETINOIN40MGCAPSULE; ORAL Prescription Yes AB
ACCUTANE ISOTRETINOIN20MGCAPSULE; ORAL Prescription Yes AB


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